drugset / Trial / NCT03825809

Nonopioid Analgesia After Labral Surgery

NCT03825809

Phase 2/3 Recruiting 100 enrolled Henry Ford Health System
RandomizedParallel-groupSingle-blindTreatment

Summary

This is a randomized, single blinded, standard of care controlled clinical trial. This project aims to compare postoperative pain control in patients in two treatment arms of rotator cuff repair: a treatment group given a nonopioid pain control regimen, and a standard of care control group given standard opioid pain control regimen

Timeline

Start
2019-01-22
Primary completion
2020-01-20
Completion
2020-05-20

Drugs

EvaluationDrugModalityDoseRoute
Subject Acetaminophen Small molecule
Subject Celecoxib Other / unclassified
Subject Diazepam Small molecule
Subject Gabapentin Small molecule
Comparator Hydrocodone Unknown
Subject Ketorolac Other / unclassified